Metabolite

KNApSAcK Entry

id C00026024
Name Reticuline N-oxide
CAS RN 71657-63-1
Standard InChI InChI=1S/C19H23NO5/c1-20(23)7-6-13-10-19(25-3)17(22)11-14(13)15(20)8-12-4-5-18(24-2)16(21)9-12/h4-5,9-11,15,21-22H,6-8H2,1-3H3/t15-,20?/m0/s1
Standard InChI (Main Layer) InChI=1S/C19H23NO5/c1-20(23)7-6-13-10-19(25-3)17(22)11-14(13)15(20)8-12-4-5-18(24-2)16(21)9-12/h4-5,9-11,15,21-22H,6-8H2,1-3H3

Cluster

Phytochemical cluster
KCF-S cluster No. 896

Link

ChEMBL

By standard InChI CHEMBL1402907
By standard InChI Main Layer CHEMBL1402907

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
eudicotyledons 1

Family

family name count
Menispermaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Pachygone ovata Miers 152360 Menispermaceae eudicotyledons Viridiplantae

Human Protein / Gene in interaction

7 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P10253 Lysosomal alpha-glucosidase Hydrolase CHEMBL1402907 CHEMBL1614076 (1)
1 / 1
Q9HBX9 Relaxin receptor 1 Relaxin receptor CHEMBL1402907 CHEMBL1613930 (1)
0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein CHEMBL1402907 CHEMBL1794584 (1)
2 / 0
Q9Y256 CAAX prenyl protease 2 U48 CHEMBL1402907 CHEMBL1794566 (1)
0 / 0
P10636 Microtubule-associated protein tau Unclassified protein CHEMBL1402907 CHEMBL1614421 (1)
4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL1402907 CHEMBL1613914 (1)
0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme CHEMBL1402907 CHEMBL2114738 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (4)

KEGG disease name UniProt
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)